Cyclization of N-alkylazinium cations with bifunctional nucleophiles. 16. σ-adducts of quinoxalinium salts with amines,alcohols, and enolates and their role in cyclizations with β-dicarbonyl compounds |
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Authors: | Charushin V. N. Ponizovskii M. G. Chupakhin O. N. Sidorov E. O. Sosonkin I. M. |
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Affiliation: | (1) S. M. Kirov Ural Polytechnic Institute, Sverdlovsk |
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Abstract: | In the reaction of N-methylquinoxalinium iodide with acetylacetone at –30 °C, the formation of 3-acetyl-2,4-dimethyl-3a,4,9,9a-tetrahydrofuro[2,3-b]quinoxaline has been recorded by 1H NMR spectroscopy, this being a regioisomer of the 3-acetyl-2,9-dimethyl-3a,4,9,9a-tetrahydro[2,3-b]quinoxaline formed in this reaction at temperatures above –10 °C. -Adducts of the N-methylquinoxalinium cation with alcohols, amines, and -diketones have also been identified, and their role in cyclizations leading to the annelation of a furan ring is discussed.For Communication 15, see [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 669–677, May, 1985. |
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